Iqbal Muhammad Haseeb, Revana Faratiana Jeanne Rosine, Pradel Emeline, Gribova Varvara, Mamchaoui Kamel, Coirault Catherine, Meyer Florent, Boulmedais Fouzia
Université de Strasbourg, CNRS, Institut Charles Sadron, UPR 22, Strasbourg Cedex 2, 67034, France.
Centre de Recherche en Biomédecine de Strasbourg, Institut National de la Santé et de la Recherche Médicale, UMR 1121, Biomatériaux et Bioingénierie, Strasbourg Cedex, 67085, France.
ACS Nano. 2022 Dec 27;16(12):20034-20043. doi: 10.1021/acsnano.2c06329. Epub 2022 Oct 27.
The engineering of skeletal muscle tissue, a highly organized structure of myotubes, is promising for the treatment of muscle injuries and muscle diseases, for replacement, or for pharmacology research. Muscle tissue development involves differentiation of myoblasts into myotubes with parallel orientation, to ultimately form aligned myofibers, which is challenging to achieve on flat surfaces. In this work, we designed hydrogen-bonded tannic acid/collagen layer-by-layer (TA/COL LbL) nanofilms using a simple brushing method to address this issue. In comparison to films obtained by dipping, brushed TA/COL films showed oriented COL fibers of 60 nm diameter along the brushing direction. Built at acidic pH due to COL solubility, TA/COL films released TA in physiological conditions with a minor loss of thickness. After characterization of COL fibers' orientation, human myoblasts (C25CL48) were seeded on the oriented TA/COL film, ended by COL. After 12 days in a differentiation medium without any other supplement, human myoblasts were able to align on brushed TA/COL films and to differentiate into long aligned myotubes (from hundreds of μm up to 1.7 mm length) thanks to two distinct properties: (i) the orientation of COL fibers guiding myoblasts' alignment and (ii) the TA release favoring the differentiation. This simple and potent brushing process allows the development of anisotropic tissues which can be used for studies of drug discovery and screening or the replacement of damaged tissue.
骨骼肌组织是一种由肌管组成的高度有组织结构,其工程化在治疗肌肉损伤和肌肉疾病、组织替代或药理学研究方面具有广阔前景。肌肉组织发育涉及成肌细胞分化为平行排列的肌管,最终形成排列整齐的肌纤维,而在平面上实现这一过程具有挑战性。在这项工作中,我们采用简单的刷涂方法设计了氢键结合的单宁酸/胶原蛋白逐层(TA/COL LbL)纳米薄膜来解决这一问题。与通过浸渍获得的薄膜相比,刷涂的TA/COL薄膜在刷涂方向上显示出直径为60 nm的取向COL纤维。由于COL在酸性pH下具有溶解性,TA/COL薄膜在生理条件下释放TA,且厚度损失较小。在对COL纤维的取向进行表征后,将人成肌细胞(C25CL48)接种在以COL结尾的取向TA/COL薄膜上。在无任何其他补充物的分化培养基中培养12天后,人成肌细胞能够在刷涂的TA/COL薄膜上排列,并分化为长的排列整齐的肌管(长度从数百微米到1.7毫米),这得益于两个独特的特性:(i)COL纤维的取向引导成肌细胞排列;(ii)TA的释放有利于分化。这种简单而有效的刷涂过程能够开发出各向异性组织,可用于药物发现和筛选研究或受损组织的替代。